Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where authors phrase all words ' Farber, C' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 9 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Runte, M; Farber, C; Lich, C; Zeschnigk, M; Buchholz, T; Smith, A; Van Maldergem, L; Burger, J; Muscatelli, F; Gillessen-Kaesbach, G; Horsthemke, B; Buiting, K
      Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15

      EUROPEAN JOURNAL OF HUMAN GENETICS
    2. Dorr, S; Midro, AT; Farber, C; Giannakudis, J; Hansmann, I
      Construction of a detailed physical and transcript map of the candidate region for Russell-Silver syndrome on chromosome 17q23-q24

      GENOMICS
    3. Farber, C; Gross, S; Neesen, J; Buiting, K; Horsthemke, B
      Identification of a testis-specific gene (C15orf2) in the Prader-Willi syndrome region on chromosome 15

      GENOMICS
    4. Buiting, K; Farber, C; Kroisel, P; Wagner, K; Brueton, L; Robertson, ME; Lich, C; Horsthemke, B
      Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselling

      CLINICAL GENETICS
    5. Farber, C; Dittrich, B; Buiting, K; Horsthemke, B
      The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletion

      HUMAN MOLECULAR GENETICS
    6. BUITING K; DITTRICH B; GROSS S; LICH C; FARBER C; BUCHHOLZ T; SMITH E; REIS A; BURGER J; NOTHEN MM; BARTHWITTE U; JANSSEN B; ABELIOVICH D; LERER I; VANDENOUWELAND AMW; HALLEY DJJ; SCHRANDERSTUMPEL C; SMEETS H; MEINECKE P; MALCOLM S; GARDNER A; LALANDE M; NICHOLLS RD; FRIEND K; SCHULZE A; MATTHIJS G; KOKKONEN H; HILBERT P; VANMALDERGEM L; GLOVER G; CARBONELL P; WILLEMS P; GILLESSENKAESBACH G; HORSTHEMKE B
      SPORADIC IMPRINTING DEFECTS IN PRADER-WILLI-SYNDROME AND ANGELMAN-SYNDROME - IMPLICATIONS FOR IMPRINT-SWITCH MODELS, GENETIC-COUNSELING, AND PRENATAL-DIAGNOSIS

      American journal of human genetics
    7. YOUNES A; CABANILLAS F; MCLAUGHLIN PW; HAGEMEISTER FB; FARBER C; SARRIS A; PATE O; MYERS J; PORTLOCK C
      PRELIMINARY EXPERIENCE WITH PACLITAXEL FOR THE TREATMENT OF RELAPSED AND REFRACTORY HODGKINS-DISEASE

      Annals of oncology
    8. SAMAL PK; FARBER C; FAROOQUEE NA; RAWAT DS
      POLYANDRY IN A CENTRAL HIMALAYAN COMMUNITY - AN ECOCULTURAL ANALYSIS

      Man in India
    9. BAUMANN E; BETHELL T; BIALY H; DUESBERG PH; FARBER C; GESHEKTER CL; JOHNSON PE; MAVER RW; SCHOCH R; STEWART GT; STROHMAN RC; THOMAS CA
      AIDS PROPOSAL

      Science


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/10/20 alle ore 01:02:23